66934-12-1Relevant academic research and scientific papers
DNA-binding studies and biological activities of new nitrosubstituted acyl thioureas
Tahir, Shaista,Badshah, Amin,Hussain, Raja Azadar,Tahir, Muhammad Nawaz,Tabassum, Saira,Patujo, Jahangir Ali,Rauf, Muhammad Khawar
, p. 215 - 225 (2015)
Four new nitrosubstituted acylthioureas i.e. 1-acetyl-3-(4-nitrophenyl)thiourea (TU1), 1-acetyl-3-(2-methyl-4-nitrophenyl)thiourea (TU2), 1-acetyl-3-(2-methoxy-4-nitrophenyl)thiourea (TU3) and 1-acetyl-3-(4-chloro-3-nitrophenyl)thiourea (TU4) have been sy
Synthesis of N-benzothiazol-2-yl-amides by Pd-catalyzed C(sp2)-H functionalization
Wang, Jun-Ke,Zong, Ying-Xiao,Wang, Xi-Cun,Hu, Yu-Lai,Yue, Guo-Ren
, p. 1376 - 1380 (2015/10/28)
A catalytic synthesis of N-benzothiazol-2-yl-amides from 1-acyl-3-(phenyl)thioureas was achieved in the presence of a palladium catalyst through the C(sp2)-H functionalization/C-S bond formation. This synthetic methodology can produce various N
REACTIONS OF ISOTHIOCYANATES AND ISOCYANATES WITH SOME SILYLATED NITROGEN-CONTAINING NUCLEOPHILES
Gonda, Josef,Antalova, Zuzana
, p. 685 - 694 (2007/10/02)
Aryl isothiocyanates and arylisocyanates react with N,O-bis(trimethylsilyl)acetamide to give N-methyl-N'-arylthioureas and ureas.Also nucleophilic additions of other aprotic nucleophiles (e.g.N-trimethylsilylimidazole, N-trimethylsilylpiperidine and N-trimethylsilylmorpholine) to the N=C=X (X=O,S) group were investigated.
